Incidental Mutation 'R5968:Tcstv5'
ID 470708
Institutional Source Beutler Lab
Gene Symbol Tcstv5
Ensembl Gene ENSMUSG00000078537
Gene Name Tcstv family member 5
Synonyms B020031M17Rik
MMRRC Submission 043249-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # R5968 (G1)
Quality Score 191
Status Not validated
Chromosome 13
Chromosomal Location 120410893-120412342 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to C at 120411618 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000137705 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080505] [ENSMUST00000180768]
AlphaFold Q3UT11
Predicted Effect probably benign
Transcript: ENSMUST00000080505
SMART Domains Protein: ENSMUSP00000111142
Gene: ENSMUSG00000078537

DomainStartEndE-ValueType
Pfam:DUF1438 7 157 8.2e-93 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000180768
SMART Domains Protein: ENSMUSP00000137705
Gene: ENSMUSG00000078537

DomainStartEndE-ValueType
Pfam:DUF1438 7 157 8.2e-93 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 93.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc10 T C 17: 46,621,077 (GRCm39) T978A probably benign Het
Adcy9 A G 16: 4,116,606 (GRCm39) L638P probably damaging Het
Adgrf2 A G 17: 43,026,063 (GRCm39) probably null Het
Anxa6 T C 11: 54,885,167 (GRCm39) I461V probably damaging Het
Arap1 T C 7: 101,043,945 (GRCm39) L668P probably damaging Het
Ces2e G T 8: 105,659,627 (GRCm39) G498W probably damaging Het
Crb1 A G 1: 139,170,739 (GRCm39) C823R probably damaging Het
Ehmt1 C T 2: 24,726,469 (GRCm39) R772H probably damaging Het
Enpep A G 3: 129,074,587 (GRCm39) L721S probably benign Het
Flii T G 11: 60,611,038 (GRCm39) I464L probably benign Het
Gm57858 T C 3: 36,064,840 (GRCm39) Q511R probably benign Het
Gtf2h3 C T 5: 124,722,360 (GRCm39) T121I probably benign Het
Ift172 T C 5: 31,418,828 (GRCm39) E1162G probably damaging Het
Meioc A G 11: 102,566,657 (GRCm39) S758G probably damaging Het
Ndst1 A C 18: 60,846,148 (GRCm39) S54A probably benign Het
Ndufaf8 G T 11: 119,990,055 (GRCm39) E56* probably null Het
Ndufb7 A G 8: 84,293,530 (GRCm39) D28G probably benign Het
Or1e16 T C 11: 73,286,018 (GRCm39) M277V possibly damaging Het
Or2a25 A G 6: 42,888,480 (GRCm39) I8V probably benign Het
Prkg1 A T 19: 30,570,324 (GRCm39) F443I probably damaging Het
Pspc1 C T 14: 57,001,693 (GRCm39) R227H probably benign Het
Ptpn21 A G 12: 98,677,149 (GRCm39) Y120H probably damaging Het
Runx1t1 A T 4: 13,841,890 (GRCm39) probably null Het
Ryr3 T C 2: 112,477,394 (GRCm39) D4449G probably benign Het
Sacs C A 14: 61,427,078 (GRCm39) A159E probably damaging Het
Slc16a14 T C 1: 84,890,226 (GRCm39) I360V possibly damaging Het
Thop1 A G 10: 80,911,393 (GRCm39) D93G probably benign Het
Tmem92 A C 11: 94,669,564 (GRCm39) M85R probably benign Het
Ttn T C 2: 76,688,017 (GRCm39) probably benign Het
Zdhhc5 T C 2: 84,524,719 (GRCm39) probably null Het
Zfp335 T C 2: 164,734,314 (GRCm39) H1291R probably damaging Het
Zfp957 C T 14: 79,451,496 (GRCm39) C101Y probably damaging Het
Other mutations in Tcstv5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4700:Tcstv5 UTSW 13 120,411,378 (GRCm39) missense probably benign 0.01
R5345:Tcstv5 UTSW 13 120,411,384 (GRCm39) missense probably damaging 0.98
R5762:Tcstv5 UTSW 13 120,411,501 (GRCm39) missense probably benign
R6221:Tcstv5 UTSW 13 120,411,534 (GRCm39) missense probably damaging 0.99
R7080:Tcstv5 UTSW 13 120,411,270 (GRCm39) missense probably benign
R9438:Tcstv5 UTSW 13 120,411,363 (GRCm39) missense probably benign 0.01
RF010:Tcstv5 UTSW 13 120,411,582 (GRCm39) missense probably benign 0.00
Predicted Primers
Posted On 2017-03-31